Rice GM - Search Results

1

Microdissection-based high-resolution genomic array analysis of two patients with cytogenetically identical interstitial deletions of chromosome 1q but distinct clinical phenotypes.

Rice GM, Qi Z, Selzer R, Richmond T, Thompson K, Pauli RM, Yu J. Rice GM, et al. Am J Med Genet A. 2006 Aug 1;140(15):1637-43. doi: 10.1002/ajmg.a.31349. Am J Med Genet A. 2006. PMID: 16835927

2

Clinical and molecular characterization of overlapping interstitial Xp21-p22 duplications in two unrelated individuals.

Thorson L, Bryke C, Rice G, Artzer A, Schilz C, Israel J, Huber S, Laffin J, Raca G. Thorson L, et al. Am J Med Genet A. 2010 Apr;152A(4):904-15. doi: 10.1002/ajmg.a.33340. Am J Med Genet A. 2010. PMID: 20358600

3

Phenotype of FOXP2 haploinsufficiency in a mother and son.

Rice GM, Raca G, Jakielski KJ, Laffin JJ, Iyama-Kurtycz CM, Hartley SL, Sprague RE, Heintzelman AT, Shriberg LD. Rice GM, et al. Am J Med Genet A. 2012 Jan;158A(1):174-81. doi: 10.1002/ajmg.a.34354. Epub 2011 Nov 21. Am J Med Genet A. 2012. PMID: 22106036 Free PMC article.

4

Mild clinical presentation in a child with prenatally diagnosed 45,X/47,XX,+18 mosaicism.

Tyler CT, Rice GM, Grady M, Raca G. Tyler CT, et al. Among authors: rice gm. Am J Med Genet A. 2009 Nov;149A(11):2588-92. doi: 10.1002/ajmg.a.33084. Am J Med Genet A. 2009. PMID: 19876897 No abstract available.

5

Improved clinical outcome following liver transplant in patients with ethylmalonic encephalopathy.

Tam A, AlDhaheri NS, Mysore K, Tessier ME, Goss J, Fernandez LA, D'Alessandro AM, Schwoerer JS, Rice GM, Elsea SH, Scaglia F. Tam A, et al. Among authors: rice gm. Am J Med Genet A. 2019 Jun;179(6):1015-1019. doi: 10.1002/ajmg.a.61104. Epub 2019 Mar 12. Am J Med Genet A. 2019. PMID: 30864297 Free PMC article.

6

Prenatal presentation of Mabry syndrome with congenital diaphragmatic hernia and phenotypic overlap with Fryns syndrome.

Reynolds KK, Juusola J, Rice GM, Giampietro PF. Reynolds KK, et al. Among authors: rice gm. Am J Med Genet A. 2017 Oct;173(10):2776-2781. doi: 10.1002/ajmg.a.38379. Epub 2017 Aug 17. Am J Med Genet A. 2017. PMID: 28817240

7

A case of congenitally absent left internal carotid artery: vascular malformations in 22q11.2 deletion syndrome.

Johnson MD, Gentry LR, Rice GM, Mount DL. Johnson MD, et al. Among authors: rice gm. Cleft Palate Craniofac J. 2010 May;47(3):314-7. doi: 10.1597/09-061.1. Cleft Palate Craniofac J. 2010. PMID: 19860531

8

The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia.

Dimmock DP, Trapane P, Feigenbaum A, Keegan CE, Cederbaum S, Gibson J, Gambello MJ, Vaux K, Ward P, Rice GM, Wolff JA, O'Brien WE, Fang P. Dimmock DP, et al. Among authors: rice gm. Am J Med Genet A. 2008 Nov 15;146A(22):2885-90. doi: 10.1002/ajmg.a.32527. Am J Med Genet A. 2008. PMID: 18925679 Free PMC article.

9

Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population.

Kuhl A, van Calcar S, Baker M, Seroogy CM, Rice G, Scott Schwoerer J. Kuhl A, et al. Genet Med. 2017 Mar;19(3):352-356. doi: 10.1038/gim.2016.104. Epub 2016 Aug 11. Genet Med. 2017. PMID: 27513192 Free article.

10

Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia.

Dimmock D, Trapane P, Feigenbaum A, Keegan CE, Cederbaum S, Gibson J, Gambello MJ, Vaux K, Ward P, Rice GM, Wolff JA, O'Brien WE, Fang P. Dimmock D, et al. Among authors: rice gm. Hum Genet. 2009 Aug;126(2):341. Hum Genet. 2009. PMID: 19694025 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

56 results

Search Page